Valdivia Bryan, Perez Pablo, Cortez Alvaro
Internal Medicine, Saint Joseph Clinic PC, Dalton, USA.
Family Medicine, Augusta University Medical College of Georgia, Chatsworth, USA.
Cureus. 2024 Dec 29;16(12):e76594. doi: 10.7759/cureus.76594. eCollection 2024 Dec.
Hairy cell leukemia (HCL) is a rare, chronic B-cell malignancy with an indolent course that typically responds well to purine nucleoside analogs, such as cladribine. We present the case of a 74-year-old woman with nearly three decades of recurrent HCL, marked by multiple relapses and significant toxicities to various treatments, including purine analogs, BRAF inhibitors, BTK inhibitors, a cytoreductive agent, and the monoclonal antibody rituximab. Despite severe allergic reactions and intolerances to standard therapies, the patient achieved multiple remissions. This case underscores the challenges in managing treatment-resistant HCL and highlights the need for personalized treatment strategies in patients with relapsed disease and drug toxicities.
毛细胞白血病(HCL)是一种罕见的慢性B细胞恶性肿瘤,病程进展缓慢,通常对嘌呤核苷类似物(如克拉屈滨)反应良好。我们报告了一例74岁女性患者,患有复发性HCL近三十年,其特点是多次复发,并且对包括嘌呤类似物、BRAF抑制剂、BTK抑制剂、一种细胞减灭剂和单克隆抗体利妥昔单抗在内的各种治疗产生显著毒性。尽管对标准疗法存在严重过敏反应和不耐受,但该患者仍实现了多次缓解。该病例强调了治疗耐药性HCL的管理挑战,并突出了对于复发疾病和药物毒性患者采用个性化治疗策略的必要性。